eudamed_udi
Primary ID: 06975447582041
Unspecified Brand (UDI 06975447582041)
Manufactured by Igenesis(Shanghai)Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06975447582041
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 106-0044-01) is a medical device manufactured by Igenesis(Shanghai)Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0105070506 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 106-0044-01
- Product Code / EMDN
- W0105070506
- Device Name
- Dengue virus/Chikungunya virus/Zika virus Diagnostic Kit (PCR-Fluorescence)
- Database Sync Date
- 2026-08-09 16:30:38
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Igenesis(Shanghai)Co.,Ltd..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975447582041.
What classification code is assigned to this device?
This device is registered under product classification code W0105070506.
Similar Classification Devices (W0105070506)
Other Devices by Igenesis(Shanghai)Co.,Ltd.
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